Hereditary motor and sensory neuropathy associated with cerebellar atrophy (HMSNCA): Clinical and neuropathological features of a Japanese family

Author:

Sekijima Y,Ohara S,Nakagawa S,Tabata K,Yoshida K,Ishigame H,Shimizu Y,Yanagisawa N

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference22 articles.

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2. Friedreich's ataxia: autosomal recessive disease caused by an intronic GAA triplet repeat expansion;Campuzano;Science,1996

3. Dyck PJ, Chance P, Lebo R, Carney JA. Hereditary motor and sensory neuropathies. In: Dyck PJ, Thomas PK, editors. Peripheral neuropathy. Philadelphia: WB Saunders, 1993:1094–136.

4. Genetic data and natural history of Friedreich's disease: a study of 80 Italian patients;Filla;J Neurol,1990

5. Autosomal dominant spinocerebellar ataxia with sensory axonal neuropathy (SCA4): clinical description and genetic localization to chromosome 16q22.1;Flanigan;Am J Hum Genet,1996

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